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引用本文:徐雪梅1,张小平2,姚丹丹2,王如伟2.HPLC测定灯盏花素缓释胶囊含量[J].中国现代应用药学,2009,(7):596-598.
XU Xuemei1, ZHANG Xiaoping2, YAO Dandan2, WANG Ruwei2.Determination of Scutellarin Brevisapin Sustained-Release Capsules by HPLC[J].Chin J Mod Appl Pharm(中国现代应用药学),2009,(7):596-598.
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HPLC测定灯盏花素缓释胶囊含量
徐雪梅1,张小平2,姚丹丹2,王如伟2
作者单位
徐雪梅1,张小平2,姚丹丹2,王如伟2  
摘要:
目的建立灯盏花素缓释胶囊中野黄芩苷的高效液相色谱法(HPLC)含量测定方法。方法采用高效液相色谱法,C18柱色谱柱(4.6 mm ×150 mm,5 μm),柱温30 ℃;进样量10 μL,流动相:甲醇-四氢呋喃-0.1%磷酸溶液(14∶14∶72),流速1.0 mL·min-1;检测波长335 nm。结果野黄芩苷在24.45~293.46 μg·mL-1范围内,峰面积与浓度的线性关系良好(r=0.999 9),野黄芩苷平均回收率为101.5%,RSD为3.616%。结论该方法简便准确,重现性好,可用于灯盏花素缓释胶囊的质量控制。
关键词:  灯盏花素缓释胶囊  高效液相色谱法  野黄芩苷  含量测定
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Determination of Scutellarin Brevisapin Sustained-Release Capsules by HPLC
XU Xuemei1, ZHANG Xiaoping2, YAO Dandan2, WANG Ruwei2
Abstract:
OBJECTIVE To develop an HPLC method of scutellarin in brevisapin sustained-release capsules. METHODS C18(4.6 mm ×150 mm, 5 μm) column with temperature of 30 ℃ was used. The mobile phase was the mixed solution of methanol- tetrahydrofuran-0.1% phosphoric acid (14∶14∶72) with the flow rate of 1.0 mL·min-1. Determination wavelength was 335 nm and the sample injected volume was 10 μL. RESULTS A good linearity of scutellarin was in the range of 24.45-293.46 μg·mL-1. The average recovery of scutellarin was 101.5% with RSD=3.616%. CONCLUSION The method is simple, accurate, and can be used for the quality control of brevisapin sustained-release capsules.
Key words:  brevisapin sustained-release capsules  HPLC  scutellarin  content determination
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